Insecta: Lepidoptera)
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Moths Light a Way? by John Pickering, Tori Staples and Rebecca Walcott
SOUTHERN LEPIDOPTERISTS NEWS VOLUME 38 NO4. (2016), PG. 331 SAVE ALL SPECIES – MOTHS LIGHT A WAY? BY JOHN PICKERING, TORI STAPLES AND REBECCA WALCOTT Abstract -- What would it take to save all species from snakes, and stinging insects, they pose no health risk. extinction? A new initiative, Save all species, plans to Moths are an exceedingly species-rich group, for which answer this question and provide the tools we need to do the diversity at a terrestrial site will typically exceed any so by 2050. Here we consider the merits and problems other taxon except for beetles. Because moth larvae are associated with inventorying moths to help decide which restricted in their diet to specific host taxa, differences in terrestrial areas to protect. We compare the the assemblages of resident moth species could reflect scientifically-described moth fauna of the British Isles differences across sites in plants and other hosts. If which, with 2,441 species, is taxonomically complete, that’s true, we may be able to use moth inventories as with 11,806 described species from North America north efficient proxies to compare surrounding plant of Mexico, the fauna of which is not fully described. As communities. a percentage of the described moth fauna, there are fewer “macro” moths (Geometroidea, Drepanoidea, Inventorying moths presents challenges, notably, Noctuoidea, Bombycoidea, Lasiocampidae) in the sampling smaller species, describing thousands of British Isles (34.9%) than those known for the United species new to science, and identifying specimens States and Canada (46.1%). We present data on 1,254 accurately. Our experience is that we can identify 99% species for an intensively-studied site in Clarke County, of moths from digital images to species, species-groups, Georgia and consider whether species in the British Isles which contain species of similar appearance, or are generally smaller than ones in Georgia. -
Modular Structure, Sequence Diversification and Appropriate
www.nature.com/scientificreports OPEN Modular structure, sequence diversifcation and appropriate nomenclature of seroins produced Received: 17 July 2018 Accepted: 14 February 2019 in the silk glands of Lepidoptera Published: xx xx xxxx Lucie Kucerova1, Michal Zurovec 1,2, Barbara Kludkiewicz1, Miluse Hradilova3, Hynek Strnad3 & Frantisek Sehnal1,2 Seroins are small lepidopteran silk proteins known to possess antimicrobial activities. Several seroin paralogs and isoforms were identifed in studied lepidopteran species and their classifcation required detailed phylogenetic analysis based on complete and verifed cDNA sequences. We sequenced silk gland-specifc cDNA libraries from ten species and identifed 52 novel seroin cDNAs. The results of this targeted research, combined with data retrieved from available databases, form a dataset representing the major clades of Lepidoptera. The analysis of deduced seroin proteins distinguished three seroin classes (sn1-sn3), which are composed of modules: A (includes the signal peptide), B (rich in charged amino acids) and C (highly variable linker containing proline). The similarities within and between the classes were 31–50% and 22.5–25%, respectively. All species express one, and in exceptional cases two, genes per class, and alternative splicing further enhances seroin diversity. Seroins occur in long versions with the full set of modules (AB1C1B2C2B3) and/or in short versions that lack parts or the entire B and C modules. The classes and the modular structure of seroins probably evolved prior to the split between Trichoptera and Lepidoptera. The diversity of seroins is refected in proposed nomenclature. Te silk spun by caterpillars is a composite material based on two protein agglomerates that have been known for centuries as fbroin and sericin. -
Lepidoptera of North America 5
Lepidoptera of North America 5. Contributions to the Knowledge of Southern West Virginia Lepidoptera Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Lepidoptera of North America 5. Contributions to the Knowledge of Southern West Virginia Lepidoptera by Valerio Albu, 1411 E. Sweetbriar Drive Fresno, CA 93720 and Eric Metzler, 1241 Kildale Square North Columbus, OH 43229 April 30, 2004 Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Cover illustration: Blueberry Sphinx (Paonias astylus (Drury)], an eastern endemic. Photo by Valeriu Albu. ISBN 1084-8819 This publication and others in the series may be ordered from the C.P. Gillette Museum of Arthropod Diversity, Department of Bioagricultural Sciences and Pest Management Colorado State University, Fort Collins, CO 80523 Abstract A list of 1531 species ofLepidoptera is presented, collected over 15 years (1988 to 2002), in eleven southern West Virginia counties. A variety of collecting methods was used, including netting, light attracting, light trapping and pheromone trapping. The specimens were identified by the currently available pictorial sources and determination keys. Many were also sent to specialists for confirmation or identification. The majority of the data was from Kanawha County, reflecting the area of more intensive sampling effort by the senior author. This imbalance of data between Kanawha County and other counties should even out with further sampling of the area. Key Words: Appalachian Mountains, -
Butterflies and Moths of Gwinnett County, Georgia, United States
Heliothis ononis Flax Bollworm Moth Coptotriche aenea Blackberry Leafminer Argyresthia canadensis Apyrrothrix araxes Dull Firetip Phocides pigmalion Mangrove Skipper Phocides belus Belus Skipper Phocides palemon Guava Skipper Phocides urania Urania skipper Proteides mercurius Mercurial Skipper Epargyreus zestos Zestos Skipper Epargyreus clarus Silver-spotted Skipper Epargyreus spanna Hispaniolan Silverdrop Epargyreus exadeus Broken Silverdrop Polygonus leo Hammock Skipper Polygonus savigny Manuel's Skipper Chioides albofasciatus White-striped Longtail Chioides zilpa Zilpa Longtail Chioides ixion Hispaniolan Longtail Aguna asander Gold-spotted Aguna Aguna claxon Emerald Aguna Aguna metophis Tailed Aguna Typhedanus undulatus Mottled Longtail Typhedanus ampyx Gold-tufted Skipper Polythrix octomaculata Eight-spotted Longtail Polythrix mexicanus Mexican Longtail Polythrix asine Asine Longtail Polythrix caunus (Herrich-Schäffer, 1869) Zestusa dorus Short-tailed Skipper Codatractus carlos Carlos' Mottled-Skipper Codatractus alcaeus White-crescent Longtail Codatractus yucatanus Yucatan Mottled-Skipper Codatractus arizonensis Arizona Skipper Codatractus valeriana Valeriana Skipper Urbanus proteus Long-tailed Skipper Urbanus viterboana Bluish Longtail Urbanus belli Double-striped Longtail Urbanus pronus Pronus Longtail Urbanus esmeraldus Esmeralda Longtail Urbanus evona Turquoise Longtail Urbanus dorantes Dorantes Longtail Urbanus teleus Teleus Longtail Urbanus tanna Tanna Longtail Urbanus simplicius Plain Longtail Urbanus procne Brown Longtail -
Preliminary Studies of the Biodiversity in Garay Cue
ISSN 2313-0504 1(11)2014 PARAGUAY BIODIVERSITY PARAGUAY BIODIVERSITÄT Lasionota dispar (Kerremans, 1903) foto: U. Drechsel Asunción, Agosto 2014 Paraguay Biodiversidad 1(11) 51-60 Asunción, Agosto 2014 Preliminary studies of the Biodiversity in Garay Cue “Reserva Natural Privada Cerrados del Tagatiya” Ulf Drechsel* Abstract: Impressions during four short visits in recent years in the "Reserva Natural Privada Cerrados del Tagatiya " in the Estancia Garay Cué are represented by photographic documentation. Resumen: Impresiones durante cuatro visitas cortas en los últimos años en la " Reserva Natural Privada Cerrados del Tagatiya " en la Estancia Garay Cué están representados por una documentación fotográfica. Zusammenfassung: Eindruecke von vier Kurzbesuchen in den letzten Jahren in der “Reserva Natural Privada Cerrados del Tagatiya” in der Estancia Garay Cué werden durch fotographische Dokumentation dargestellt. Key words: Paraguay, Garay Cue, biodiversity In the northeast of the Department of Concepción in the eastern region of Paraguay is located the Estancia Garay Cué with an area of about 18,800 ha, of which form about 5,200 ha the " Reserva Natural Privada Cerrados del Tagatiya", a nature reserve under private management. The estancia is located between two national parks, the "Parque Nacional Paso Bravo" in the Northeast and the "Parque Nacional Serrania de San Luis" in the West and include semi-deciduous forests, gallery forests and various types of Cerrado. During four short visits from December 2012 to June 2013 could be obtained first impressions of the existing biodiversity and photos of plants and animals were made. Special attention was paid to the most neglected invertebrate fauna, as this is the main part of biodiversity with thousands of species, many of them still unknown to science. -
Lepidoptera, Endromidae) in China
A peer-reviewed open-access journal ZooKeys 127: 29–42 (2011)The genusAndraca (Lepidoptera, Endromidae) in China... 29 doi: 10.3897/zookeys.127.928 RESEARCH artICLE www.zookeys.org Launched to accelerate biodiversity research The genus Andraca (Lepidoptera, Endromidae) in China with descriptions of a new species Xing Wang1,†, Ling Zeng2,‡, Min Wang2,§ 1 Department of Entomology, South China Agricultural University, Guangzhou, Guangdong 510640, P.R. China. Present address: Institute of Entomology, College of Biosafety Science and Technology, Hunan Agricul- tural University, Changsha 410128 Hunan, China; and Provincial Key Laboratory for Biology and Control of Plant Diseases and Insect Pests, Changsha 410128, Hunan, China 2 Department of Entomology, South China Agricultural University, Guangzhou, Guangdong 510640, P.R. China † urn:lsid:zoobank.org:author:F8727887-0014-42D4-BA68-21B3009E8C7F ‡ urn:lsid:zoobank.org:author:7981BF0E-D1F8-43CA-A505-72DBBA140023 § urn:lsid:zoobank.org:author:D683614E-1F58-4CA8-9D80-B23BD41947A2 Corresponding author: Ling Zeng ([email protected]) Academic editor: N. Wahlberg | Received 21 January 2011 | Accepted 15 August 2011 | Published 8 September 2011 urn:lsid:zoobank.org:pub:33D4BBFB-4B7D-4BBC-B34C-17D2E7F99F67 Citation: Wang X, Zeng L, Wang M (2011) The genus Andraca (Lepidoptera, Endromidae) in China with descriptions of a new species. ZooKeys 127: 29–42. doi: 10.3897/zookeys.127.928 Abstract The six species of the genus Andraca Walker hitherto known from China are reviewed, and a new species, A. gongshanensis, sp. n., described from Yunnan Province, China. Adults and male genitalia of all exam- ined species are illustrated, together with a distributional map. A key to all seven Chinese Andraca species is provided. -
ILLUSTRATIONS of MOTHS in TAIWAN, 1-5 by B. S. Chang
142 BOOK REVIEW TROPICAL LEPIDOPTERJ Tropical Lepidoptera, 4(2): 142 BOOK REVIEW ILLUSTRATIONS OF MOTHS IN TAIWAN, 1-5 by B. S. Chang Vol. 1: Sphingidae, Ratardidae. Epipyropidae, Drepanidae, Cyclidiidae, Thyatiridae, Epicopeiidae, Callidulidae. Lasiocampidae. EupterotidJ Bombycidae, Brahmaeidae, Agaristidae [Noctuidae, part]. 242 pp, 271 col. fig., col. cover. 1989. (paper only) Vol. 2: Arctiidae, Hypsidae [Noctuidae, part], Limacodidae, Notodontidae. 310 pp, 356 col. fig., col. cover. 1989. Vol. 3: Geometridae [1]. Oenochrominae, Geometrinae, Sterrhinae, Larentiinae. 350 pp, 405 col. fig., col. cover. 1989. Vol. 4: Geometridae [2]. Ennominae. 480 pp, 684 col. fig., col. cover. 1990. Vol. 5: Noctuidae [1]. 366 pp. 572 col. fig., col. cover. 1991. (paper only) 1989-91. Taiwan Museum, Taipei. All are 21 x 18.5 cm. (elongate) In Chinese; Latin names. Price for each is S35.00 paper, S42.00 cloth. Available from Flora & Fauna Books, P. O. Box 15718, Gainesville, FL 32604 (plus S2 shipping each, or 55 per set). This series of small, full-color books is the result of a lifetime of with 706 species illustrated out of the 791 recorded for Taiwan. TlJ collecting by retired Taiwan high school teacher B. S. Chang. Until color figures are all excellent but many of the wing venation drawing 1991, 5 volumes were completed, but the second part of the Noctuidae are very faintly reproduced in the books. has unfortunately been halted by the untimely death of the author. It is Overall, the books are one of the unique treatments of Lepidoptera ii not known if a manuscript is available for the eventual completion of the world. -
Acoustic Communication in the Nocturnal Lepidoptera
Chapter 6 Acoustic Communication in the Nocturnal Lepidoptera Michael D. Greenfield Abstract Pair formation in moths typically involves pheromones, but some pyra- loid and noctuoid species use sound in mating communication. The signals are generally ultrasound, broadcast by males, and function in courtship. Long-range advertisement songs also occur which exhibit high convergence with commu- nication in other acoustic species such as orthopterans and anurans. Tympanal hearing with sensitivity to ultrasound in the context of bat avoidance behavior is widespread in the Lepidoptera, and phylogenetic inference indicates that such perception preceded the evolution of song. This sequence suggests that male song originated via the sensory bias mechanism, but the trajectory by which ances- tral defensive behavior in females—negative responses to bat echolocation sig- nals—may have evolved toward positive responses to male song remains unclear. Analyses of various species offer some insight to this improbable transition, and to the general process by which signals may evolve via the sensory bias mechanism. 6.1 Introduction The acoustic world of Lepidoptera remained for humans largely unknown, and this for good reason: It takes place mostly in the middle- to high-ultrasound fre- quency range, well beyond our sensitivity range. Thus, the discovery and detailed study of acoustically communicating moths came about only with the use of electronic instruments sensitive to these sound frequencies. Such equipment was invented following the 1930s, and instruments that could be readily applied in the field were only available since the 1980s. But the application of such equipment M. D. Greenfield (*) Institut de recherche sur la biologie de l’insecte (IRBI), CNRS UMR 7261, Parc de Grandmont, Université François Rabelais de Tours, 37200 Tours, France e-mail: [email protected] B. -
The Mcguire Center for Lepidoptera and Biodiversity
Supplemental Information All specimens used within this study are housed in: the McGuire Center for Lepidoptera and Biodiversity (MGCL) at the Florida Museum of Natural History, Gainesville, USA (FLMNH); the University of Maryland, College Park, USA (UMD); the Muséum national d’Histoire naturelle in Paris, France (MNHN); and the Australian National Insect Collection in Canberra, Australia (ANIC). Methods DNA extraction protocol of dried museum specimens (detailed instructions) Prior to tissue sampling, dried (pinned or papered) specimens were assigned MGCL barcodes, photographed, and their labels digitized. Abdomens were then removed using sterile forceps, cleaned with 100% ethanol between each sample, and the remaining specimens were returned to their respective trays within the MGCL collections. Abdomens were placed in 1.5 mL microcentrifuge tubes with the apex of the abdomen in the conical end of the tube. For larger abdomens, 5 mL microcentrifuge tubes or larger were utilized. A solution of proteinase K (Qiagen Cat #19133) and genomic lysis buffer (OmniPrep Genomic DNA Extraction Kit) in a 1:50 ratio was added to each abdomen containing tube, sufficient to cover the abdomen (typically either 300 µL or 500 µL) - similar to the concept used in Hundsdoerfer & Kitching (1). Ratios of 1:10 and 1:25 were utilized for low quality or rare specimens. Low quality specimens were defined as having little visible tissue inside of the abdomen, mold/fungi growth, or smell of bacterial decay. Samples were incubated overnight (12-18 hours) in a dry air oven at 56°C. Importantly, we also adjusted the ratio depending on the tissue type, i.e., increasing the ratio for particularly large or egg-containing abdomens. -
Report-VIC-Croajingolong National Park-Appendix A
Croajingolong National Park, Victoria, 2016 Appendix A: Fauna species lists Family Species Common name Mammals Acrobatidae Acrobates pygmaeus Feathertail Glider Balaenopteriae Megaptera novaeangliae # ~ Humpback Whale Burramyidae Cercartetus nanus ~ Eastern Pygmy Possum Canidae Vulpes vulpes ^ Fox Cervidae Cervus unicolor ^ Sambar Deer Dasyuridae Antechinus agilis Agile Antechinus Dasyuridae Antechinus mimetes Dusky Antechinus Dasyuridae Sminthopsis leucopus White-footed Dunnart Felidae Felis catus ^ Cat Leporidae Oryctolagus cuniculus ^ Rabbit Macropodidae Macropus giganteus Eastern Grey Kangaroo Macropodidae Macropus rufogriseus Red Necked Wallaby Macropodidae Wallabia bicolor Swamp Wallaby Miniopteridae Miniopterus schreibersii oceanensis ~ Eastern Bent-wing Bat Muridae Hydromys chrysogaster Water Rat Muridae Mus musculus ^ House Mouse Muridae Rattus fuscipes Bush Rat Muridae Rattus lutreolus Swamp Rat Otariidae Arctocephalus pusillus doriferus ~ Australian Fur-seal Otariidae Arctocephalus forsteri ~ New Zealand Fur Seal Peramelidae Isoodon obesulus Southern Brown Bandicoot Peramelidae Perameles nasuta Long-nosed Bandicoot Petauridae Petaurus australis Yellow Bellied Glider Petauridae Petaurus breviceps Sugar Glider Phalangeridae Trichosurus cunninghami Mountain Brushtail Possum Phalangeridae Trichosurus vulpecula Common Brushtail Possum Phascolarctidae Phascolarctos cinereus Koala Potoroidae Potorous sp. # ~ Long-nosed or Long-footed Potoroo Pseudocheiridae Petauroides volans Greater Glider Pseudocheiridae Pseudocheirus peregrinus -
Contributions Toward a Lepidoptera (Psychidae, Yponomeutidae, Sesiidae, Cossidae, Zygaenoidea, Thyrididae, Drepanoidea, Geometro
Contributions Toward a Lepidoptera (Psychidae, Yponomeutidae, Sesiidae, Cossidae, Zygaenoidea, Thyrididae, Drepanoidea, Geometroidea, Mimalonoidea, Bombycoidea, Sphingoidea, & Noctuoidea) Biodiversity Inventory of the University of Florida Natural Area Teaching Lab Hugo L. Kons Jr. Last Update: June 2001 Abstract A systematic check list of 489 species of Lepidoptera collected in the University of Florida Natural Area Teaching Lab is presented, including 464 species in the superfamilies Drepanoidea, Geometroidea, Mimalonoidea, Bombycoidea, Sphingoidea, and Noctuoidea. Taxa recorded in Psychidae, Yponomeutidae, Sesiidae, Cossidae, Zygaenoidea, and Thyrididae are also included. Moth taxa were collected at ultraviolet lights, bait, introduced Bahiagrass (Paspalum notatum), and by netting specimens. A list of taxa recorded feeding on P. notatum is presented. Introduction The University of Florida Natural Area Teaching Laboratory (NATL) contains 40 acres of natural habitats maintained for scientific research, conservation, and teaching purposes. Habitat types present include hammock, upland pine, disturbed open field, cat tail marsh, and shallow pond. An active management plan has been developed for this area, including prescribed burning to restore the upland pine community and establishment of plots to study succession (http://csssrvr.entnem.ufl.edu/~walker/natl.htm). The site is a popular collecting locality for student and scientific collections. The author has done extensive collecting and field work at NATL, and two previous reports have resulted from this work, including: a biodiversity inventory of the butterflies (Lepidoptera: Hesperioidea & Papilionoidea) of NATL (Kons 1999), and an ecological study of Hermeuptychia hermes (F.) and Megisto cymela (Cram.) in NATL habitats (Kons 1998). Other workers have posted NATL check lists for Ichneumonidae, Sphecidae, Tettigoniidae, and Gryllidae (http://csssrvr.entnem.ufl.edu/~walker/insect.htm). -
Traditional Consumption of and Rearing Edible Insects in Africa, Asia and Europe
Critical Reviews in Food Science and Nutrition ISSN: 1040-8398 (Print) 1549-7852 (Online) Journal homepage: http://www.tandfonline.com/loi/bfsn20 Traditional consumption of and rearing edible insects in Africa, Asia and Europe Dele Raheem, Conrado Carrascosa, Oluwatoyin Bolanle Oluwole, Maaike Nieuwland, Ariana Saraiva, Rafael Millán & António Raposo To cite this article: Dele Raheem, Conrado Carrascosa, Oluwatoyin Bolanle Oluwole, Maaike Nieuwland, Ariana Saraiva, Rafael Millán & António Raposo (2018): Traditional consumption of and rearing edible insects in Africa, Asia and Europe, Critical Reviews in Food Science and Nutrition, DOI: 10.1080/10408398.2018.1440191 To link to this article: https://doi.org/10.1080/10408398.2018.1440191 Accepted author version posted online: 15 Feb 2018. Published online: 15 Mar 2018. Submit your article to this journal Article views: 90 View related articles View Crossmark data Full Terms & Conditions of access and use can be found at http://www.tandfonline.com/action/journalInformation?journalCode=bfsn20 CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION https://doi.org/10.1080/10408398.2018.1440191 Traditional consumption of and rearing edible insects in Africa, Asia and Europe Dele Raheema,b, Conrado Carrascosac, Oluwatoyin Bolanle Oluwoled, Maaike Nieuwlande, Ariana Saraivaf, Rafael Millanc, and Antonio Raposog aDepartment for Management of Science and Technology Development, Ton Duc Thang University, Ho Chi Minh City, Vietnam; bFaculty of Applied Sciences, Ton Duc Thang University, Ho Chi Minh City, Vietnam;